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Items: 1 to 50 of 97

1.

Transgenerational Inheritance of Familial Lipomyelomeningocele.

Larrew T, Eskandari R, Holden KR, Chen A, Spellicy CJ, Jones JR, Lee JA, Lyons MJ.

J Child Neurol. 2017 Dec;32(14):1118-1122. doi: 10.1177/0883073817736701.

PMID:
29129155
2.

Feasibility of developing a pediatric telehealth network in Honduras with international consultation support.

Brooks M, Holden KR, Durón RM, McElligott JT, Summer A.

Rural Remote Health. 2017 Apr-Jun;17(2):3965. doi: 10.22605/RRH3965. Epub 2017 May 31.

3.

Clinical Features and Neurologic Complications of Children Hospitalized With Chikungunya Virus in Honduras.

Samra JA, Hagood NL, Summer A, Medina MT, Holden KR.

J Child Neurol. 2017 Jul;32(8):712-716. doi: 10.1177/0883073817701879. Epub 2017 May 1.

PMID:
28459170
4.

Importance of genetic testing in global health during the evaluation of familial microcephaly.

Molinero I, Broman-Fulks J, Lyons MJ, Matheus MG, Chaubey A, DuPont BR, Friez MJ, Skinner SA, Holden KR.

Clin Case Rep. 2016 Aug 26;4(10):968-971. eCollection 2016 Oct.

5.

A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.

Smith JA, Holden KR, Friez MJ, Jones JR, Lyons MJ.

Am J Med Genet A. 2016 Dec;170(12):3313-3318. doi: 10.1002/ajmg.a.37945. Epub 2016 Aug 29.

PMID:
27570168
6.
7.

The influence of traditional and complementary and alternative medicine on medication adherence in Honduras.

Catalino MP, Durón RM, Bailey JN, Holden KR.

Altern Ther Health Med. 2015 May-Jun;21(3):26-35.

PMID:
26026142
8.

Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.

Matheus MG, Lehman RK, Bonilha L, Holden KR.

J Child Neurol. 2015 Oct;30(12):1664-8. doi: 10.1177/0883073815578524. Epub 2015 Apr 21.

PMID:
25900139
9.

Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicism.

Dwivedi AC, Lyons MJ, Kwiatkowski K, Bartel FO, Friez MJ, Holden KR, Fung ET, DuPont BR.

Mol Cytogenet. 2014 Dec 4;7(1):93. doi: 10.1186/s13039-014-0093-4. eCollection 2014.

10.

Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment.

Smith AW, Holden KR, Dwivedi A, Dupont BR, Lyons MJ.

J Child Neurol. 2015 Mar;30(4):517-21. doi: 10.1177/0883073814545113. Epub 2014 Oct 7.

PMID:
25296922
11.

Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.

Mooneyham KA, Holden KR, Cathey S, Dwivedi A, Dupont BR, Lyons MJ.

Am J Med Genet A. 2014 Nov;164A(11):2887-91. doi: 10.1002/ajmg.a.36708. Epub 2014 Aug 13.

PMID:
25123844
12.

Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion.

Dean SJ, Holden KR, Dwivedi A, Dupont BR, Lyons MJ.

Pediatr Neurol. 2014 Jun;50(6):636-9. doi: 10.1016/j.pediatrneurol.2014.01.055. Epub 2014 Feb 10.

PMID:
24725350
13.

Heads you win, tails you lose: measuring head circumference.

Holden KR.

Dev Med Child Neurol. 2014 Aug;56(8):705. doi: 10.1111/dmcn.12449. Epub 2014 Mar 24. No abstract available.

14.

Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation.

Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG.

J Child Neurol. 2014 Aug;29(8):NP13-7. doi: 10.1177/0883073813492384. Epub 2013 Jul 21.

PMID:
23877478
15.

β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.

Hayflick SJ, Kruer MC, Gregory A, Haack TB, Kurian MA, Houlden HH, Anderson J, Boddaert N, Sanford L, Harik SI, Dandu VH, Nardocci N, Zorzi G, Dunaway T, Tarnopolsky M, Skinner S, Holden KR, Frucht S, Hanspal E, Schrander-Stumpel C, Mignot C, Héron D, Saunders DE, Kaminska M, Lin JP, Lascelles K, Cuno SM, Meyer E, Garavaglia B, Bhatia K, de Silva R, Crisp S, Lunt P, Carey M, Hardy J, Meitinger T, Prokisch H, Hogarth P.

Brain. 2013 Jun;136(Pt 6):1708-17. doi: 10.1093/brain/awt095. Epub 2013 May 17.

16.

Novel mutation in Sjogren-Larsson syndrome is associated with divergent neurologic phenotypes.

Davis K, Holden KR, S'Aulis D, Amador C, Matheus MG, Rizzo WB.

J Child Neurol. 2013 Oct;28(10):1259-65. doi: 10.1177/0883073812460581. Epub 2012 Oct 3.

17.

Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.

Lyons MJ, Fuller JD, Montoya Mdel C, DuPont BR, Holden KR.

J Child Neurol. 2013 Apr;28(4):524-6. doi: 10.1177/0883073812446309. Epub 2012 Jun 29.

PMID:
22752474
18.

Neuroscience curriculum changes and outcomes: medical university of South Carolina, 2006 to 2010.

Holden KR, Cooper SL, Wong JG.

Neurologist. 2012 Jul;18(4):190-5. doi: 10.1097/NRL.0b013e3182613e1b.

PMID:
22735242
19.

Seizures and X-linked intellectual disability.

Stevenson RE, Holden KR, Rogers RC, Schwartz CE.

Eur J Med Genet. 2012 May;55(5):307-12. doi: 10.1016/j.ejmg.2012.01.017. Epub 2012 Feb 8. Review.

20.

LIS1 duplication: expanding the phenotype.

Lockrow JP, Holden KR, Dwivedi A, Matheus MG, Lyons MJ.

J Child Neurol. 2012 Jun;27(6):791-5. doi: 10.1177/0883073811425972. Epub 2011 Dec 21.

PMID:
22190508
21.

Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2).

Burruss DM, Wood TC, Espinoza L, Dwivedi A, Holden KR.

J Child Neurol. 2012 Jun;27(6):786-90. doi: 10.1177/0883073811425860. Epub 2011 Dec 21.

PMID:
22190500
22.

Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature.

Dukes-Rimsky L, Guzauskas GF, Holden KR, Griggs R, Ladd S, Montoya Mdel C, DuPont BR, Srivastava AK.

Am J Med Genet A. 2011 Sep;155A(9):2146-53. doi: 10.1002/ajmg.a.34137. Epub 2011 Aug 10.

23.

Autism in two females with duplications involving Xp11.22-p11.23.

Edens AC, Lyons MJ, Duron RM, Dupont BR, Holden KR.

Dev Med Child Neurol. 2011 May;53(5):463-6. doi: 10.1111/j.1469-8749.2010.03909.x. Epub 2011 Mar 21.

24.

Reduction in rate of epilepsy from neurocysticercosis by community interventions: the Salamá, Honduras study.

Medina MT, Aguilar-Estrada RL, Alvarez A, Durón RM, Martínez L, Dubón S, Estrada AL, Zúniga C, Cartagena D, Thompson A, Ramirez E, Banegas L, Osorio JR, Delgado-Escueta AV, Collins JS, Holden KR.

Epilepsia. 2011 Jun;52(6):1177-85. doi: 10.1111/j.1528-1167.2010.02945.x. Epub 2011 Jan 28.

25.

Natural history of Christianson syndrome.

Schroer RJ, Holden KR, Tarpey PS, Matheus MG, Griesemer DA, Friez MJ, Fan JZ, Simensen RJ, Strømme P, Stevenson RE, Stratton MR, Schwartz CE.

Am J Med Genet A. 2010 Nov;152A(11):2775-83. doi: 10.1002/ajmg.a.33093.

26.

Adult convulsive status epilepticus in the developing country of Honduras.

Skinner HJ, Dubon-Murcia SA, Thompson AR, Medina MT, Edwards JC, Nicholas JS, Holden KR.

Seizure. 2010 Jul;19(6):363-7. doi: 10.1016/j.seizure.2010.05.007. Epub 2010 Jun 15.

27.

Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.

Lyons MJ, Duron R, Molinero I, Sangiuolo F, Holden KR.

Pediatr Neurol. 2010 May;42(5):365-8. doi: 10.1016/j.pediatrneurol.2010.01.014.

PMID:
20399394
28.

United States head circumference growth reference charts: birth to 21 years.

Rollins JD, Collins JS, Holden KR.

J Pediatr. 2010 Jun;156(6):907-913.e2. doi: 10.1016/j.jpeds.2010.01.009. Epub 2010 Mar 20.

PMID:
20304425
29.

Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder.

Geer JS, Skinner SA, Goldin E, Holden KR.

Pediatr Neurol. 2010 Mar;42(3):223-6. doi: 10.1016/j.pediatrneurol.2009.10.002.

30.

Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.

Pollard LM, Williams NR, Espinoza L, Wood TC, Spector EB, Schroer RJ, Holden KR.

J Child Neurol. 2010 Aug;25(8):954-60. doi: 10.1177/0883073809351984. Epub 2009 Dec 18.

PMID:
20023066
31.

Utilization of blood spot testing for metabolic-genetic disorders in Honduras: is it time for newborn screening?

Slaughter JL, Espinoza L, Molinero I, Wood TC, Duron C, Flores A, Porter R, Tomashitis K, Holden KR.

J Child Neurol. 2010 Mar;25(3):306-11. doi: 10.1177/0883073809339059. Epub 2009 Oct 21.

PMID:
19850562
32.

Pediatric convulsive status epilepticus in Honduras, Central America.

Molinero MR, Holden KR, Rodriguez LC, Collins JS, Samra JA, Shinnar S.

Epilepsia. 2009 Oct;50(10):2314-9. doi: 10.1111/j.1528-1167.2009.02266.x. Epub 2009 Aug 19.

33.

A novel mutation in type II methemoglobinemia.

Hudspeth MP, Joseph S, Holden KR.

J Child Neurol. 2010 Jan;25(1):91-3. doi: 10.1177/0883073809336136. Epub 2009 May 26.

PMID:
19471045
34.

Adherence and complementary and alternative medicine use among Honduran people with epilepsy.

Durón RM, Medina MT, Nicolás O, Varela FE, Ramírez F, Battle SJ, Thompson A, Rodríguez LC, Oseguera C, Aguilar-Estrada RL, Pietsch-Escueta S, Collins JS, Holden KR.

Epilepsy Behav. 2009 Apr;14(4):645-50. doi: 10.1016/j.yebeh.2009.01.022. Epub 2009 Feb 4.

PMID:
19435580
35.

FIRST: a practical approach to the causes and management of febrile seizures.

Mohebbi MR, Holden KR, Butler IJ.

J Child Neurol. 2008 Dec;23(12):1484-8. doi: 10.1177/0883073808319317. Review.

PMID:
19073858
36.

A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.

Gregory ML, Guzauskas GF, Edgar TS, Clarkson KB, Srivastava AK, Holden KR.

J Child Neurol. 2008 Dec;23(12):1433-8. doi: 10.1177/0883073808320754.

PMID:
19073849
37.

The modified Atkins diet: a potential treatment for developing countries.

Kossoff EH, Dorward JL, Molinero MR, Holden KR.

Epilepsia. 2008 Sep;49(9):1646-7. doi: 10.1111/j.1528-1167.2008.01580_6.x. No abstract available.

38.

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.

Cantagrel V, Silhavy JL, Bielas SL, Swistun D, Marsh SE, Bertrand JY, Audollent S, Attié-Bitach T, Holden KR, Dobyns WB, Traver D, Al-Gazali L, Ali BR, Lindner TH, Caspary T, Otto EA, Hildebrandt F, Glass IA, Logan CV, Johnson CA, Bennett C, Brancati F; International Joubert Syndrome Related Disorders Study Group, Valente EM, Woods CG, Gleeson JG.

Am J Hum Genet. 2008 Aug;83(2):170-9. doi: 10.1016/j.ajhg.2008.06.023.

39.

Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.

Amador C, Mathews AM, Del Carmen Montoya M, Laughridge ME, Everman DB, Holden KR.

J Child Neurol. 2008 Aug;23(8):901-5. doi: 10.1177/0883073808317730.

PMID:
18660473
40.

Finding new etiologies of mental retardation and hypotonia: X marks the spot.

Rogers RC, Stevenson RE, Simensen RJ, Holden KR, Schwartz CE.

Dev Med Child Neurol. 2008 Feb;50(2):104-11. doi: 10.1111/j.1469-8749.2007.02022.x. Epub 2008 Jan 7. Review.

41.

Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.

Giurgiutiu DV, Espinoza LM, Wood TC, DuPont BR, Holden KR.

J Child Neurol. 2008 Jan;23(1):112-7. doi: 10.1177/0883073807307979.

PMID:
18184946
42.

Early onset alpha-mannosidosis with slow progression in three Hispanic males.

Lyons MJ, Wood T, Espinoza L, Stensland HM, Holden KR.

Dev Med Child Neurol. 2007 Nov;49(11):854-7. Erratum in: Dev Med Child Neurol. 2008 Jan;50(1):32.

43.

What do future (female) pediatricians value?

Smith AW, Glenn RC, Williams V, Kostova F, Holden KR, Gillespie CF, Boutwell B, Richard GV, Maria BL; Association of Medical School Pediatric Department Chairs, Inc.

J Pediatr. 2007 Nov;151(5):443-4, 444.e1-2. No abstract available.

PMID:
17961680
44.

Expansion of the deletion 13q syndrome phenotype: a case report.

Lance EI, DuPont BR, Holden KR.

J Child Neurol. 2007 Sep;22(9):1124-7.

PMID:
17890413
45.

Developing a neurology training program in Honduras: a joint project of neurologists in Honduras and the World Federation of Neurology.

Medina MT, Munsat T, Portera-Sánchez A, Durón RM, Becker CA, Holden KR; WFN Education Committee.

J Neurol Sci. 2007 Feb 15;253(1-2):7-17. Epub 2006 Dec 22.

PMID:
17188302
46.

Unusual phenotypic expression of an XLRS1 mutation in X-linked juvenile retinoschisis.

Dodds JA, Srivastava AK, Holden KR.

J Child Neurol. 2006 Apr;21(4):331-3.

PMID:
16900931
47.

A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.

Addison PK, Berry V, Holden KR, Espinal D, Rivera B, Su H, Srivastava AK, Bhattacharya SS.

Mol Vis. 2006 Jul 20;12:791-5.

48.

The "slurp" test: bedside evaluation of bulbar muscle fatigue.

Hudspeth MP, Holden KR, Crawford TO.

Pediatrics. 2006 Aug;118(2):e530-3. Epub 2006 Jul 17.

PMID:
16847079
49.

Sturge-Weber syndrome variant with atypical intracranial findings: case report.

Yallapragada AV, Cure JK, Holden KR.

J Child Neurol. 2006 Feb;21(2):155-7.

PMID:
16566882
50.

Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts.

Vajsar J, Zhang W, Dobyns WB, Biggar D, Holden KR, Hawkins C, Ray P, Olney AH, Burson CM, Srivastava AK, Schachter H.

Neuromuscul Disord. 2006 Feb;16(2):132-6. Epub 2006 Jan 19.

PMID:
16427280

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